Dispers-reactive dyes containing acetoxymethylsulfone or vinylsulfone and their process

ABSTRACT

The present invention relates to water insoluble disperse-reactive dyes expressed by the formula (3) and (4) and to their preparation, (3) (4) wherein each of Ar 1  and Ar 2  represents aryl or benzothiazole group, and each of R, R 1 , R 2 , and R 3  independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group.

BACKGROUND OF THE INVENTION

[0001] 1. Field of the Invention

[0002] The invention relates to new disperse-reactive dyes and to their preparation. More specifically, the present invention relates to the disperse-reactive dyes with acetoxyethylsulfone and vinylsulfone as reactive groups represented by the formula (1) and (2),

AcOCH₂CH₂SO₂—Ar₁—NH₂  (1)

H₂C═CHSO₂—Ar₂—NH₂  (2)

[0003] Wherein each of Ar₁ and Ar₂ is aryl or benzothiazole.

[0004] According to the invention, there are provided water insoluble disperse-reactive dyes expressed by the formula (3) and (4).

[0005] wherein each of Ar₁ and Ar₂ represents aryl or benzothiazole group, and each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group.

[0006] 2. Description of the Related Art

[0007] For dyeing of wool, silk, nylon and polyurethane, there have been generally employed water-soluble dyes such as acid dyes, metal complex dyes and reactive dyes. The largest number of acid and metal complex dyes are constituted azo dyes, which are capable of releasing some carcinogenic aromatic amines as a result of the reductive cleavage of azo bonds. It has been also reported that azo dyes can be metabolically cleaved by enzymatic reduction in the human organs.

[0008] In 1995, the German law on harmful substances listed 20 hazardous aromatic amines, and prohibited the import as well as selling of textiles and goods dyed with dyestuff based on cleavable those amines. Recently, the environmental protection are becoming important concern, therefore the use of metal complex dyes including heavy metals has been strictly regulated. The conventional acid and metal complex dyes have high water solubility, and they cause dyeing wastewater containing a high concentration of residual dyes. And also those dyes give poor washing fastness. The conventional reactive dyes exhibit very good washing fastness by forming a covalent bond between fiber and dye. However the dyeing with reactive dyes is carried out under alkali condition, it may cause degradation of wool or silk fiber.

[0009] In 1960, the water-insoluble disperse-reactive dyes were introduced by ICI (Imperial Chemical Industries Ltd.) as Procinyl dyestuff.

[0010] In present several disperse-reactive dyes are commercially available and the research is continuously progressing.

SUMMARY OF THE INVENTION

[0011] An object of this invention is to provide water-insoluble disperse-reactive dyes which have reactive group to form covalent bond with fibers, and do not include carcinogenic harmful amines or heavy metals.

[0012] As a result of continuous studies in order to prepare water-insoluble disperse-reactive dyes of high brilliance and fastness, especially washing fastness, the inventors completed this invention by synthesizing water-insoluble disperse-reactive dyes having acetoxyethylsulfone and vinylsulfone as reactive group.

DETAILED DESCRIPTION OF THE INVENTION

[0013] This invention provides water-insoluble disperse-reactive dyes represented by the general formula (3a), (3b), (4a) and (4b), which is combined with reactive groups such as β-acetoxyethylsulfone or vinylsulfone group,

[0014] wherein each of A and B represents hydrogen, alkyl or alkoxy group, and each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group.

[0015] In accordance with one aspect of the present invention, there is provided a process for the production of water-insoluble disperse-reactive dyes which are suitable for the dyeing of wool, silk, nylon, polyurethane and mixed-fibers.

[0016] According to this invention, the disperse-reactive dyes having β-acetoxyethylsulfone or vinylsulfone group are prepared as follows;

[0017] (a) diazotizing each of 4-aminophenyl-β-acetoxyethylsulfone, 2-amino-5-(β-acetoxyethylsulfone)benzothiazole, 2,5-substituted-aminophenyl-4-vinylsulfone or 2-amino-5-vinylsulfonebenzothiazole expressed by the following formula 5, 7, 10 and 11; and

[0018] (b) coupling with the coupler of formula 6 keeping in acidic condition.

[0019] The individual preparation methods are described more in detail as shown in Scheme 1, 2, 3, 5 and 6.

[0020] wherein each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group.

[0021] According to the above Scheme 1, the preparation method of disperse-reactive dye expressed by the formula 3a is explained in more detail.

[0022] 4-Aminophenyl-β-acetoxyethylsulfone of formula 5 is diazotized. A generally available diazotization method is adapted, which means that after dispersing the 4-aminophenyl-β-acetoxyethylsulfone in water at 0-5° C. and the diazotization reaction is carried with the addition of concentrated hydrochloric acid and NaNO₂. And the coupler solution under acidic condition is cooled down below 5° C. to carry out the coupling reaction with the diazotized compound at 0-5° C. And then the prepared coupler solution is slowly added to the diazotized solution at 0-5° C., stirred, neutralized with alkali solution, preferably to the pH 6.5 and filtered to obtain a final product.

[0023] As a raw material, 4-aminophenyl-β-acetoxyethylsulfone compound presented by the formula 5 is synthesized by the simple reaction of 4-acetaminophenyl-β-hydroxyethylsulfone with a mixture of hydrogen chloride and acetic acid (Korea Patent No 198829).

[0024] The preparation method of the disperse-reactive dyes having 2-amino-5-(β-acetoxyethylsulfone)benzothiazole of formula 3b is expressed in more detail the following Scheme 2,

[0025] wherein each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group.

[0026] According to the present invention, the disperse-reactive dyes of formula 3b may be prepared in various preparing methods, which is differentiated by starting material used.

[0027] The above Scheme 2 represents 2-amino-5-(β-acetoxyethylsulfone)benzothiazole of formula 7 is used as a starting material, on the other hand 2-amino-5-(β-hydroxyethylsulfone)benzothiazole of formula 8 can also be used as a starting material as shown in the following Scheme 3,

[0028] wherein each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group.

[0029] The preparation method of the Scheme 2 is described in more detail. 2-Amino-5-(β-acetoxyethylsulfone)benzothiazole of formula 7 is dispersed at 5-10° C. in acid mixture (6 parts acetic acid: 1 part propionic acid) with nitrosylsulfuric acid to carry out diazotization. The solution of coupler of formula 6 in acid mixture is cooled down at 5-10° C., and then this solution is slowly added to the diazotized solution to carry out the coupling reaction. The coupling solution is stirred, adjusted to pH 5 with NaOAc and isolated by filtration to get disperse-reactive dyes having a wide range of colors.

[0030] As shown in the following Scheme 4, the 2-amino-5-(β-acetoxyethylsulfone)benzothiazole as a raw material of the formula 7 is prepared by reacting 4-aminophenyl-β-acetoxyethylsulfone of formula 5 with KSCN and Br₂ in acetic acid.

[0031] Another method to prepare the disperse-reactive dye of formula 3b is presented in the above Scheme 3. To obtain the dyestuff of formula 3b, the disperse-reactive dyes syntesized by:

[0032] (a) diazotizing 2-amino-5-(β-hydroxyethylsulfone)benzothiazole of formula 8;

[0033] (b) coupling with the couplers of formula 6 keeping in acidic condition at 5-10° C.; and

[0034] (c) reacting with acetic anhydride of the compound of formula 9 at 80-90° C.

[0035] In this reaction, the compound of formula 9 should be separated and dried before it is reacted with acetic anhydride.

[0036] Hereunder, the process for synthesizing a disperse-reactive dye presented by the formula 4a is described more in detail as shown in Scheme 5.

[0037] wherein each of A and B is a hydrogen, alkyl or alkoxy group, and each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group.

[0038] 2,5-Substituted-aminophenyl-4-vinylsulfone of formula 10 is diazotized. The diazotization is accomplished by commonly available method, for example, 2,5-substituted-aminophenyl-4-vinylsulfone is dispersed in water at 0-5° C., and the diazotization is carried out with adding of concentrated hydrochloric acid and NaNO₂. In another vessel, the solution of coupler of formula 6 prepared by using concentrated hydrochloric acid and water is cooled down below 5° C., which is slowly added to the above prepared diazotized solution at 0-5° C. to carry out the coupling reaction. This coupling solution is stirred for a while and neutralized by using alkali solution up to pH 6.5. The final disperse-reactive dye products having vinylsulfone reactive group is isolated by filtration.

[0039] The preparation method of the disperse-reactive dyes having 2-amino-5-vinylsulfone-benzothiazole of formula 4b is expressed in more detail the following formula Scheme 6,

[0040] wherein each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group.

[0041] The preparation method of the Scheme 6 is described in more detail. 2-amino-5-vinylsulfone-benzothiazole of formula 11 is dispersed at 5-10° C. in acid mixture (6 parts acetic acid: 1 part propionic acid) with nitrosylsulfuric acid to carry out diazotization. The solution of coupler of formula 6 in acid mixture is cooled down at 5-10° C., and then this solution is slowly added to the diazotized solution to carry out the coupling reaction. The coupling solution is stirred, adjusted to pH 5 with NaOAc and isolated by filtration to get disperse-reactive dyes having a wide range of colors.

[0042] The 2-amino-5-vinylsulfone-benzothiazole as a raw material of the formula 11 is prepared by reacting aminophenyl-4-vinylsulfone of formula 10(A, B=H) with KSCN and Br₂ as shown in Scheme 7.

[0043] The disperse-reactive dyes of the present invention are valuable dyestuff in case of dyeing to wool, silk, nylon, polyurethane and mixed-fibers. They cover a wide range of colors with excellent brightness and good fastness, especially washing fastness by the covalent bonds to form between dye and fiber.

[0044] The following specific examples are intended to be illustrative of the invention and should not be construed as limiting the scope of the invention as defined by appended claims.

EXAMPLES OF THE COMPOUNDS CONTAINING REACTIVE GROUPS Example 1 Preparation of 4-aminophenyl-β-acetoxyethylsulfone(5)

[0045] To 100 ml flask equipped with condenser with a balloon was added a mixture of acetic acid (60 g, 1 mol) and water (1.8 g, 0.1 mol), and then HCl gas (5.5 g, 0.15 mol) was slowly added to the reaction solution for 1.5-2 hours at 15° C. Thereafter 4-acetaminophenyl-β-hydroxyethylsulfone (24.3 g, 0.1 mol) was added to the reaction mixture and slowly heated to 70-75° C. for 1 hour and stirred 9 hours. And then the reaction mixture was cooled down to room temperature, filtered and washed with acetic acid (5 ml) twice. After drying the isolated product, it was dispersed in a mixture of ice (10 g) and water (25 ml) and neutralized with 15% Na₂CO₃ aqueous solution. The collected product was washed with water (5 ml) three times and dried to obtain 4-aminophenyl-β-acetoxyethylsulfone of formula 5 as a white solid (Yield=84.8%, purity=97.5%).

[0046]¹H NMR (300 MHz, Acetone-d₆): 1.83 (3H, s), 3.42 (2H, t), 4.30 (2H, t), 6.79 (2H, d), 7.56 (2H, d)

Example 2 Preparation of 2-amino-5-(β-acetoxyethylsulfone)benzothiazole(7)

[0047] To a dispersed solution of 4-aminophenyl-β-acetoxyethyl-sulfone (7.3 g, 0.03 mol) in acetic acid (40 ml) was added KSCN (6.6 g, 0.068 mol) at 20-25° C. and this mixture was stirred for 30 minutes. Bromine (2 ml, 0.039 mol) in acetic acid (10 ml) was added dropwise over 1 hour at 10-15° C. Thereafter the reaction mixture was heated to 35-40° C., stirred for 20 hours, and cooled down to room temperature. The reaction mixture was filtered and the residue was stirred in water (200 ml) at 85° C. After hot filtration, the filtrate was cooled down to room temperature and neutralized with 4N NaOH aqueous solution to pH 5. The precipitated product was filtered and washed with water to give pale yellow colored product 2-amino-5-(β-acetoxyethylsulfone)benzothiazole of formula 7 (Yield=60%).

[0048]¹H NMR (300 MHz, Acetone-d₆): 1.72 (3H, s), 3.57 (2H, t), 4.34 (2H, t), 7.36 (2H, br s), 7.54 (1H, d), 7.76 (1H, d), 8.22 (1H, d)

Example 3 Preparation of aminophenyl-4-vinylsulfone (10, A, B=H)

[0049] The solution of 4-aminophenyl-β-sulfatoethylsulfone (57.6 g, 0.20 mol) was dispersed in water (390 ml) at 0-5° C. In the meanwhile, the pH of the reaction mixture was maintained between 8 and 9 by the addition of 4N NaOH aqueous solution (100 ml) and stirred for 2 hours at room temperature. The reaction mixture was filtered and washed with water. The isolated product was dried to give aminophenyl-4-vinylsulfone of formula 10 (A, B=H) (Yield=81%).

[0050]¹H NMR (300 MHz, Acetone-d₆): 5.95 (1H, d), 6.19 (1H, d), 5.37 (2H, br s) 6.80 (2H, d), 6.83 (1H, d of d), 7.55 (2H, d)

Example 4 Preparation of 2,5-dimethoxyaminophenyl-4-vinylsulfone (10, A, B=HOCH₃)

[0051] The solution of 2,5-dimethoxyaminophenyl-4-β-sulfatoethylsulfone (13.6 g, 0.04 mol) in water (75 ml) was adjusted to pH 8-9 with 4N NaOH (12 ml) and heated slowly to 70-75° C. The pH of the reaction mixture was maintained between 8 and 9 by the addition of 4N NaOH aqueous solution, and stirred for 2 hours at 70-75° C. The reaction mixture was cooled down to room temperature, filtered and washed with water. The isolated product was dried to give 2,5-dimethoxyamino-phenyl-4-vinylsulfone of formula 10 (A, B=OCR) (Yield=94.7%).

[0052]¹H NMR (300 MHz, Acetone-d₆): 3.79 (3H, s), 3.82 (3H, s), 5.37 (21, br s), 5.93 (1H, d), 6.20 (1H, d), 6.50 (1H, s), 6.93 (1H, d of d), 7.17 (1H, s)

Example 5 Preparation of 2-methoxy-5-methylaminophenyl4-vinylsulfone (10, A=CH3, B=OCH₃)

[0053] The solution of 2-methoxy-5-methylaminophenyl-4-β-sulfatoethylsulfone (13.0 g, 0.04 mol) in water (65 ml) was adjusted to pH 10 with 4N NaOH (17 ml) and slowly heated to 65-70° C. The reaction mixture was stirred for 1.5 hours at 65-70° C., and then cooled down to room temperature. The precipitated product was isolated by filtration and washed with water to obtain 2-methoxy-5-methylamino phenyl-4-vinyl-sulfone of formula 10 (A=CH₃, B=OCH₃) (Yield=90.3%).

[0054]¹H NMR (300 MHz, Acetone-d₆): 2.35 (3H, s), 3.85 (3H, s), 5.26 (2H, br s), 6.00 (1H, d), 6.19 (1H, d), 6.62 (1H, s), 6.76 (1H, d of d), 7.30 (1H, s)

Example 6 Preparation of 2-amino-5-vinylsulfone-benzothiazole (11)

[0055] To a dispersed solution of aminophenyl-4-vinylsulfone (36.6 g, 0.20 mol) in acetic acid (250 ml) was added KSCN (43 g, 0.44 mol) at 20-25° C. and this mixture was stirred for 30 minutes. Bromine (11.3 ml, 0.22 mol) in acetic acid (50 ml) was added dropwise over 1 hour at 10-15° C. Thereafter the reaction mixture was heated to 35-40° C., stirred for 20 hours and cooled down to room temperature. The reaction mixture was filtered. Thereafter the filtrate was diluted with water (800 ml) and neutralized with 8N NaOH aqueous solution to pH 5. The precipitated product was filtered and washed with water to give pale yellow colored product 2-amino-5-vinylsulfone-benzothiazole of formula 11 (Yield=94.5%).

[0056]¹H NMR (300 MHz, Acetone-d₆): 5.95 (1H, d), 6.20 (1H, d), 6.79 (1H, d of d), 7.39 (2H, br s), 7.41 (1H, d), 7.60 (1H, d of d), 8.06 (1H, d)

EXAMPLES OF THE DYES Example 1

[0057] To a dispersed solution of 4-aminophenyl-β-acetoxyethyl-sulfone (7.4 g, 0.03 mol) in water (100 ml) was added 3N NaNO₂(10.5 ml, 0.032 mol), and the mixture was maintained at 0-5° C. Ice (30 g) and 35% HCl (6.5 ml, 0.075 mol) were added, and stirred for 1 hour at 0-5° C. to complete diazotization. The excess nitrous acid was destroyed by the addition of sulfamic acid. N, N-Diethylaniline (5.0 g, 0.033 mol) in water (100 ml) was maintained at the temperature 0-5° C. and added 35% HCl (10 ml, 0.115 mol) at a separate reactor. The ensuring solution was slowly added to the diazotized solution at 0-5° C. The mixture was stirred for 1 hour and adjusted to pH 6.5 with 15% Na₂CO₃ solution. The precipitated dye was collected by filtration and obtained orange colored disperse-reactive dye of formula 12 (Yield=88.5%, λ_(max)=459 nm, ε=38,100).

Example 2-7

[0058] The examples in the following Table 1 were carried out in the manner of Example 1 using the appropriate coupler (C, 0.033 mol) to obtain reactive dyes of formula 13.

TABLE 1

Ex- ample λ_(max) Yield No. Coupler(C) ε (nm) g(%) 2

37,400 463 10.3 (82.4) 3

40,800 486 13.2 (95.6) 4

33,500 510 13.1 (89.1) 5

27,000 447 11.1 (83.5) 6

27,500 490 13.1 (89.7) 7

31,600 510 13.8 (88.5)

Example 8

[0059] 4-Aminophenyl-β-acetoxyethylsulfone (7.4 g, 0.03 mol) was diazotized by the same method of example 1. 1,4-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyridine-3-carbonitrile (5.04 g, 0.031 mol) was dissolved in 0.4N NaOH solution (80 ml) and maintained at the temperature 0-5° C. The ensuring solution was slowly added to the diazotized solution at a temperature 0-5° C. and stirred for 1 hour to complete coupling. And then 15% Na₂CO₃ solution was slowly added to adjust the pH of the mixture to 6.5. The precipitated product was collected by filtration and obtained yellow colored disperse-reactive dye of formula 14 (Yield=93.6%, λ_(max)=420 nm, ε=49,000).

Example 9

[0060] To a mixture of 2-amino-5-(β-acetoxyethylsulfone)benzo-thiazole (6.0 g, 0.02 mol) in acid mixture (40 ml, 6 parts acetic: 1 part propionic acid) was added dropwise 42% HO₃SONO (4.4 ml, 0.023 mol) over 30 minutes at temperature 5-10° C. This reaction mixture was stirred for 1 hour at 5-10° C. to complete diazotization. Excess nitrous acid was destroyed by the addition of urea. A solution of N,N-diethylaniline (3.3 g, 0.022 mol) in acid mixture (33 ml) was maintained at 5-10° C., which was added slowly to the diazotized solution and then stirred for 1 hour. Sodium acetate (13.3 g) was added and stirred for 30 minutes to adjust the pH 5 of the reaction mixture. And then the reaction mixture was poured into ice-cold water (50 ml), stirred for a while, filtered and dried. The violet colored disperse-reactive dye was obtained as shown in formula 15 (Yield=98.9%, λ_(max)=527 nm, ε=25,800).

Example 10-16

[0061] The examples in the following Table 2 were carried out in the manner of example 9 using the appropriate coupler (D, 0.022 mol) to obtain disperse-reactive dyes of formula 16.

TABLE 2

Ex- ample λ_(max) Yield No. Coupler(D) ε (nm) g(%) 10

23,400 536  8.0 (84.4) 11

41,200 542  9.0 (87.1) 12

22,800 585  6.7 (61.2) 13

27,200 530  8.5 (84.8) 14

31,800 549  8.9 (81.8) 15

226,800 495 10.0 (99.0) 16

232,700 506 10.3 (98.3)

Example 17

[0062] This reaction was carried out in the manner of example 9 using 2-amino-5-(β-hydroxyethylsulfone)benzothiazole (5.2 g, 0.02 mol) instead of 2-amino-5-(β-acetoxyethylsulfone)benzothiazole, with N,N-diethyl-aniline (3.3 g, 0.022 mol) as a coupler to give the dye of formula 17.

[0063] The dried compound (1 g) of formula 17 in acetic anhydride (3.6 ml) was heated to 85-90° C. for 1.5 hours. Thereafter, this reaction mixture was cooled down to room temperature, poured into ice-cold water 80 g, and stirred for 1 hour. The produced solid product was isolated by filtration'to give dye of formula 18 (Yield=100%).

Example 18

[0064] To a dispersed solution of aminophenyl-4-vinylsulfone (3.66 g, 0.02 mol) in water (80 ml) was added 3N NaNO₂ (7 ml, 0.021 mol) and the mixture was maintained at 0-5° C. Ice (30 g) and 35% HCl (4.4 ml, 0.051 mol) were added and stirred for 1 hour at 0-5° C. to complete diazotization. Excess nitrous acid was destroyed by the addition of sulfamic acid. A solution of N,N-diethyl-m-toluidine (3.6 g, 0.022 mol) in water (65 ml) was maintained at the temperature 0-5° C. and added 35% HCl (6.5 ml, 0.075 mol) at a separate reactor.

[0065] The ensuring solution was slowly added to the diazotized solution at 0-5° C. The mixture was stirred for 1 hour and the pH of the solution was adjusted to 6.5 with 15% Na₂CO₃ solution. The precipitated dye was collected by filtration and obtained red colored disperse-reactive dye of formula 19 (Yield=95.2%, λ_(max)=467 nm, ε=34,500).

Example 19-20

[0066] The examples in the following Table 3 were carried out in the manner of example 18 using the appropriate coupler (E, 0.022 mol) to obtain disperse-reactive dyes of formula 20.

TABLE 3

Example λ_(max) No. Coupler(E) ε (nm) Yield g(%) 19

40,600 488 7.2 (90.0) 20

36,300 511 8.5 (98.8)

Example 21

[0067] Aminophenyl-4-vinylsulfone (3.66 g, 0.02 mol) was diazotized by the same method of example 18. 1,4-Dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyridine-3-carbonitrile (3.41 g, 0.021 mol) was dissolved in 0.4N NaOH solution (80 ml) and maintained at the temperature 0-5° C. The ensuring solution was slowly added to the diazotized solution at a temperature 0-5° C. and stirred for 1 hour to complete coupling reaction. And then 15% Na₂CO₃ solution was slowly added to adjust the pH of the mixture to 6.5. The precipitated product was collected by filtration and obtained yellow colored disperse-reactive dye of formula 21 (Yield=94.4%, λ_(max)=421 nm, ε=50,400).

Example 22-26

[0068] The examples in the following Table 4 are carried out in the manner of example 18 using 2,5-dimethoxyaminophenyl-4-vinylsulfone (4.86 g, 0.02 mol) as diazo compound with the appropriate coupler (F, 0.022 mol) to obtain disperse-reactive dyes of formula 22.

TABLE 4

Ex- ample λ_(max) Yield No. Coupler(F) ε (nm) g(%) 22

29,400 471 7.3 (90.5) 23

32,400 479 8.0 (95.9) 24

46,300 505 9.1 (98.9) 25

36,700 530 8.3 (84.7) 26

33,500 508 9.5 (97.5)

Example 27-31

[0069] The examples in the following Table 5 are carried out in the manner of example 18 using 2-methoxy-5-methylaminophenyl-4-vinyl-sulfone (4.6 g, 0.02 mol) as diazo compound with the appropriate coupler (G, 0.022 mol) to obtain disperse-reactive dyes of formula 23.

TABLE 5

Ex- ample λ_(max) Yield No. Coupler(G) ε (nm) g(%) 27

28,700 457 6.4 (82.7) 28

30,600 465 7.7 (96.0) 29

42,900 496 8.5 (95.7) 30

31,800 521 6.9 (66.2) 31

28,100 500 8.6 (91.3)

Example 32

[0070] To a mixture of 2-amino-5-vinylsulfone-benzothiazole (4.8 g, 0.02 mol) in acid mixture (40 ml, 6 parts acetic: 1 part propionic acid) was added dropwise 42% HO₃SONO (4.4 ml, 0.023 mol) over 30 minutes at temperature 5-10° C. This reaction mixture was stirred for 1 hour at 5-10° C. to complete diazotization. Excess nitrous acid was destroyed by the addition of urea. A solution of N,N-diethylaniline (3.3 g, 0.022 mol) in acid mixture (33 ml) was maintained at 5-10° C., which was added slowly to the diazotized solution and then stirred for 1 hour. Sodium acetate (13.3 g) was added and stirred for 30 minutes to adjust the pH 5 of the reaction mixture. And then the reaction mixture was poured into ice-cold water (50 ml), stirred for a while, filtered and dried.

[0071] The violet colored disperse-reactive dye was obtained as shown in formula 24 (Yield=74%, λ_(max)=524 nm, ε=26,000). 

What is claimed is:
 1. A disperse-reactive dye represented by the following formula 3,

wherein each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group; and Ar₁ represents aryl or benzothiazole group.
 2. A process for preparing disperse-reactive dyes represented by the formula 3, which comprises the steps of: (a) diazotizing of formula 1; and (b) coupling with a compound having the general formula 6 to obtain of formula 3, AcOCH₂CH₂SO₂—Ar₁—NH₂  (1)

wherein each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group; and Ar₁ represents aryl or benzothiazole group.
 3. A process for preparing disperse-reactive dyes represented by the formula 3b, which comprises the steps of: (a) diazotizing 2-amino-5-(β-hydroxyethylsulfone)benzothiazole of formula 8; (b) coupling with a compound having the general formula 6 to obtain of formula 9; and (c) acetylation of formula 9 with acetic anhydride to obtain of formula 3b,

wherein each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group.
 4. A disperse-reactive dye represented by the following formula 4,

wherein each of A and B represents hydrogen, alkyl or alkoxy group, and each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group, and Ar₂ represents aryl or benzothiazole group.
 5. A process for preparing disperse-reactive dyes represented by the formula 4, which comprises the steps of: (a) diazotizing of formula 2; and (b) coupling with a compound having the general formula 6 to obtain of formula 4,

wherein each of A and B represents hydrogen, alkyl or alkoxy group, and each of R, R₁, R₂, and R₃ independently represents hydrogen, alkyl, alkoxy, cyanoalkyl or aminoacetyl group, and Ar₂ represents aryl or benzothiazole group. 1-10 (Canceled)
 11. (New) A disperse-reactive dye represented by the following formula 3,

wherein AcO represents an acetoxy group; each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group; and Ar₁ represents a benzothiazole group.
 12. (New) A process for preparing disperse-reactive dyes represented by the formula 3a, which comprises the steps of: (a) diazotizing the compound of formula 5; and (b) coupling said diazotized compound with a compound having the general formula 6 to obtain the compound of formula 3a,

wherein AcO represents an acetoxy group; and each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group.
 13. (New) A process for preparing disperse-reactive dyes represented by the formula 3b, which comprises the steps of: (a) diazotizing the compound of formula 7; and (b) coupling said diazotized compound with a compound having the general formula 6 to obtain the compound of formula 3b,

wherein AcO represents an acetoxy group; and each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group.
 14. (New) A process for preparing disperse-reactive dyes represented by the formula 3b comprising the steps of: (a) diazotizing 2-amino-5-(8-hydroxyethylsulfone)benzothiazole of formula 8; (b) coupling said diazotized compound with a compound having the general formula 6 to obtain the compound of formula 9; and (c) acetylating the compound of formula 9 with acetic anhydride to obtain the compound of formula 3b,

wherein AcO represents an acetoxy group; and each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group.
 15. (New) A disperse-reactive dye represented by the following formula 4,

wherein each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group; and Ar₂ represents an aryl- or a benzothiazole group.
 16. (New) A disperse-reactive dye represented by the following formula 4a,

wherein A and B independently represents hydrogen, alkyl or alkoxy group, and each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group.
 17. (New) A disperse-reactive dye represented by the following formula 4b,

wherein each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group.
 18. (New) A process for preparing disperse-reactive dyes represented by the formula 4, which comprises the steps of: (a) diazotizing the compound of formula 2; and (b) coupling said diazotized compound with a compound having the general formula 6 to obtain the compound of formula 4, H₂C═CHSO₂—Ar₂—NH₂  (2)

wherein each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group; and Ar₂ represents an aryl- or a benzothiazole group.
 19. (New) A process for preparing disperse-reactive dyes represented by the formula 4a, which comprises the steps of: (a) diazotizing the compound of formula 10; and (b) coupling said diazotized compound with a compound having the general formula 6 to obtain the compound of formula 4a,

wherein A and B independently represents hydrogen, alkyl or alkoxy group, and each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group.
 20. (New) A process for preparing disperse-reactive dyes represented by the formula 4b, which comprises the steps of: (a) diazotizing the compound of formula 11; and (b) coupling said diazotized compound with a compound having the general formula 6 to obtain the compound of formula 4b,

wherein each of R, R₁, R₂, and R₃ independently represents a hydrogen atom, an alkyl-, an alkoxy-, a cyanoalkyl- or an aminoacetyl group. 